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2017, First edition., Methods in Enzymology, ISBN 0128095032, Volume 582.
Web Resource
2011, Advances in experimental medicine and biology, ISBN 9781441984135, Volume 712., xix, 226
Cysteine proteases expressed by pathogenic organisms play key roles in virulence including host entry, feeding and suppression of host immune responses. This... 
chemistry | Cysteine proteinases | Cysteine Proteases | Microbial enzymes | Pathogenic microorganisms | Eukaryota | Pathophysiology | Bacteria | Viruses | immunology | enzymology | Pre-clinical Medicine: Basic Sciences | Molecular Medicine | Biomedicine general | Biomedicine
Book
Journal of Immunology, ISSN 0022-1767, 10/2012, Volume 189, Issue 8, pp. 3957 - 3969
The lectin pathway of complement is an important component of innate immunity. Its activation has been thought to occur via recognition of pathogens by... 
SYSTEM | INDIVIDUALS | PATTERN-RECOGNITION MOLECULES | COMPLEMENT FACTOR-D | MBL | 3MC SYNDROME | STOICHIOMETRY | MUTATIONS | IMMUNOLOGY | IDENTIFICATION | DEFICIENCY | Craniofacial Abnormalities - immunology | Transcriptional Activation - genetics | Complement Pathway, Mannose-Binding Lectin - immunology | Blepharoptosis - genetics | Eye Abnormalities - enzymology | Mannose-Binding Protein-Associated Serine Proteases - physiology | Eye Abnormalities - immunology | Humans | Heart Defects, Congenital - immunology | Craniosynostoses - enzymology | Blepharoptosis - immunology | Developmental Disabilities - genetics | Transcriptional Activation - immunology | Strabismus - genetics | Abdominal Muscles - abnormalities | Abnormalities, Multiple - immunology | Heart Defects, Congenital - genetics | Developmental Disabilities - enzymology | Blepharoptosis - enzymology | Heart Defects, Congenital - enzymology | Mannose-Binding Protein-Associated Serine Proteases - genetics | Complement Pathway, Alternative - genetics | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Strabismus - enzymology | Abdominal Muscles - immunology | Craniosynostoses - genetics | Complement Pathway, Mannose-Binding Lectin - genetics | Cryptorchidism - enzymology | Abdominal Muscles - enzymology | Hip Dislocation, Congenital - genetics | Codon, Nonsense | Eye Abnormalities - genetics | Animals | Craniofacial Abnormalities - enzymology | Craniosynostoses - immunology | Cryptorchidism - immunology | Hip Dislocation, Congenital - immunology | Complement Pathway, Alternative - immunology | Strabismus - immunology | Abnormalities, Multiple - enzymology | Developmental Disabilities - immunology | Hip Dislocation, Congenital - enzymology | Cryptorchidism - genetics | Index Medicus | Abridged Index Medicus
Journal Article
Human Pathology, ISSN 0046-8177, 2015, Volume 49, pp. 27 - 32
Summary Complex I deficiency causes Leigh syndrome, fatal infant lactic acidosis, and neonatal cardiomyopathy. Mutations in more than 100 nuclear DNA and... 
Pathology | Metabolic disease | Lethal neonatal lactic acidosis | Whole-exome sequencing | Mitochondriopathy | Complex I deficiency | ACAD9 defect | Mitochondrial hyperplasia | Multiorgan failure | DIAGNOSIS | CARDIOMYOPATHY | PATHOLOGY | GENE | DNA | EXPRESSION | Immunohistochemistry | Fibroblasts - enzymology | Diaphragm - pathology | Mitochondria, Heart - pathology | Electron Transport Complex I - deficiency | Humans | Hyperplasia | Male | Cardiomyopathy, Hypertrophic - enzymology | Acyl-CoA Dehydrogenases - genetics | Leigh Disease - pathology | Muscle Weakness - genetics | Amino Acid Metabolism, Inborn Errors - genetics | Autopsy | DNA Mutational Analysis | Electron Transport Complex I - genetics | Fatal Outcome | Muscle Weakness - pathology | Acyl-CoA Dehydrogenases - deficiency | Amino Acid Metabolism, Inborn Errors - pathology | Kidney Tubules - pathology | Infant, Newborn | Multiple Organ Failure - pathology | Acyl-CoA Dehydrogenase - genetics | Cardiomyopathy, Hypertrophic - genetics | Genetic Predisposition to Disease | Mitochondria, Liver - pathology | Mitochondria, Heart - enzymology | Fibroblasts - pathology | Leigh Disease - genetics | Acidosis, Lactic - pathology | Cardiomyopathy, Hypertrophic - diagnosis | Mitochondrial Diseases - enzymology | Phenotype | Acyl-CoA Dehydrogenase - deficiency | Kidney Tubules - enzymology | Acidosis - diagnosis | Multiple Organ Failure - enzymology | Acidosis - genetics | Amino Acid Metabolism, Inborn Errors - enzymology | Mitochondrial Diseases - pathology | Muscle Weakness - diagnosis | Acidosis, Lactic - genetics | Cause of Death | Acidosis, Lactic - enzymology | Amino Acid Metabolism, Inborn Errors - diagnosis | DNA, Mitochondrial - genetics | Muscle Weakness - enzymology | Transfection | Mitochondrial Diseases - genetics | Mitochondria, Muscle - enzymology | Mitochondria, Muscle - pathology | Leigh Disease - enzymology | Cells, Cultured | Multiple Organ Failure - genetics | Codon, Nonsense | Mitochondria, Liver - enzymology | Multiple Organ Failure - diagnosis | Diaphragm - enzymology | Acidosis - pathology | Leigh Disease - diagnosis | Acidosis - enzymology | Mitochondrial Diseases - diagnosis | Acidosis, Lactic - diagnosis | Cardiomyopathy, Hypertrophic - pathology | Infants (Newborn) | Muscles | Genetic aspects | Mitochondrial DNA | Liver | Heart | Urine | Cytochrome | Antigens | Enzymes | Cytomegalovirus | Cardiomyopathy | Data bases | Defects | Musculoskeletal system | Rodents | Fibroblasts | Oxidation | Mutation | Metabolic disorders | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
Kidney International, ISSN 0085-2538, 11/2015, Volume 88, Issue 5, pp. 1030 - 1046
Journal Article
01/2017, ISBN 9780128093108, 486
eBook
Journal of Biological Chemistry, ISSN 0021-9258, 04/2016, Volume 291, Issue 15, pp. 7830 - 7830
Journal Article
The Journal of Biological Chemistry, ISSN 0021-9258, 3/2016, Volume 291, Issue 13, pp. 6625 - 6625
Journal Article
The Journal of Biological Chemistry, ISSN 0021-9258, 12/2015, Volume 290, Issue 51, pp. 30224 - 30224
Journal Article
Planta, ISSN 0032-0935, 1/2013, Volume 237, Issue 1, pp. 189 - 210
In recent years, there has been a significant increase in the number of completely sequenced plant genomes. The comparison of fully sequenced genomes allows... 
Enzymes | Dehydrogenases | Terminology | Algae | Evolution | Genomes | Plants | Aldehydes | Family members | Rice | Life Sciences | ALDH | Nomenclature | Forestry | Agriculture | Ecology | Gene family | Stress response | Plant Sciences | Aldehyde dehydrogenase | ARABIDOPSIS-THALIANA | OXIDATIVE STRESS | RICE ORYZA-SATIVA | TOLERANCE | ESCHERICHIA-COLI | PLANT SCIENCES | AMINOALDEHYDE DEHYDROGENASE | TOBACCO PLANTS | SUCCINIC-SEMIALDEHYDE DEHYDROGENASE | PHYSCOMITRELLA-PATENS | EXPRESSION | Sorghum - enzymology | Multigene Family | Arabidopsis - enzymology | Volvox - genetics | Zea mays - enzymology | Populus - genetics | Aldehydes - metabolism | Vitis - enzymology | Plants - enzymology | Bryopsida - genetics | Populus - enzymology | Chlamydomonas reinhardtii - genetics | Oryza - genetics | Plants - genetics | Plant Proteins - metabolism | Sorghum - genetics | Genomics - methods | Aldehyde Dehydrogenase - metabolism | Vitis - genetics | Zea mays - genetics | Genome, Plant - genetics | Volvox - enzymology | Terminology as Topic | Aldehyde Dehydrogenase - genetics | Chromosome Mapping | Plants - classification | Oryza - enzymology | Selaginellaceae - genetics | Arabidopsis - genetics | Plant Proteins - genetics | Animals | Chlamydomonas reinhardtii - enzymology | Bryopsida - enzymology | Chromosomes, Plant - genetics | Selaginellaceae - enzymology | Evolution, Molecular | Genes | Genomics | Plant genetics | Environmental health | Organic acids | Arabidopsis thaliana | Plant physiology | Physiological aspects | Genetic research | Universities and colleges | Comparative analysis | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 11/2015, Volume 290, Issue 45, pp. 26881 - 26881
Journal Article
The Journal of Biological Chemistry, ISSN 0021-9258, 8/2015, Volume 290, Issue 33, pp. 20022 - 20022
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 04/2015, Volume 290, Issue 15, pp. 9321 - 9321
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 10/2001, Volume 21, Issue 19, pp. 7691 - 7704
L-Serine is synthesized from glycolytic intermediate 3-phosphoglycerate and is an indispensable precursor for the synthesis of proteins, membrane lipids,... 
Immunohistochemistry | Brain | L-serine | Olfactory ensheathing glia | Mouse | Development | 3-Phosphoglycerate dehydrogenase | Astrocyte | In situ hybridization | development | 3-phosphoglycerate dehydrogenase | CEREBELLAR PURKINJE-CELLS | GLUCOSE DEPRIVATION | NEURON REGENERATION | brain | PRIMARY CULTURES | HIPPOCAMPAL-NEURONS | NEUROSCIENCES | FETAL MONKEY NEOCORTEX | mouse | olfactory ensheathing glia | AMINO-ACIDS | immunohistochemistry | RAT-BRAIN | BASIC-PROTEIN | astrocyte | DEVELOPMENTAL EXPRESSION | in situ hybridization | Antibody Specificity | Brain - embryology | Brain - enzymology | Serine - biosynthesis | Dendrites - ultrastructure | Stem Cells - cytology | Astrocytes - enzymology | Olfactory Bulb - embryology | Microscopy, Immunoelectron | RNA, Messenger - biosynthesis | Neuroglia - cytology | In Situ Hybridization | Organelles - ultrastructure | Stem Cells - enzymology | Gene Expression Regulation, Developmental | Organelles - enzymology | Cell Differentiation - physiology | Carbohydrate Dehydrogenases - genetics | Olfactory Bulb - cytology | Olfactory Bulb - enzymology | Astrocytes - cytology | Brain - cytology | Mice, Inbred C57BL | Neuroglia - enzymology | Synapses - enzymology | Synapses - ultrastructure | Phosphoglycerate Dehydrogenase | Cell Lineage - physiology | Animals | Dendrites - enzymology | Mice | Aging - metabolism | Carbohydrate Dehydrogenases - metabolism | Index Medicus
Journal Article
Journal Article
Nature, ISSN 0028-0836, 11/2014, Volume 515, Issue 7527, pp. 431 - 435
Journal Article